Eda Özaydın

400 total citations
24 papers, 247 citations indexed

About

Eda Özaydın is a scholar working on Surgery, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eda Özaydın has authored 24 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Surgery, 9 papers in Pulmonary and Respiratory Medicine and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eda Özaydın's work include Epilepsy research and treatment (4 papers), Metabolism and Genetic Disorders (3 papers) and Neonatal Respiratory Health Research (3 papers). Eda Özaydın is often cited by papers focused on Epilepsy research and treatment (4 papers), Metabolism and Genetic Disorders (3 papers) and Neonatal Respiratory Health Research (3 papers). Eda Özaydın collaborates with scholars based in Türkiye, United States and Italy. Eda Özaydın's co-authors include Gülşen Köse, Alev Güven, Ebru Arhan, Mehmet Gündüz, Filiz Ekici, Serdar Ceylaner, Nesibe Andıran, Belén Pérez, Tülin Revide Şaylı and Aydan Değerli̇yurt and has published in prestigious journals such as European Journal of Pediatrics, Journal of Child Neurology and Seizure.

In The Last Decade

Eda Özaydın

22 papers receiving 238 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Eda Özaydın 76 58 47 37 33 24 247
Simon Waller 98 1.3× 99 1.7× 110 2.3× 68 1.8× 18 0.5× 25 458
Tsutomu Ishizuka 175 2.3× 86 1.5× 81 1.7× 22 0.6× 28 0.8× 15 496
Hamdi Cihan Emeksiz 70 0.9× 34 0.6× 71 1.5× 18 0.5× 13 0.4× 31 291
Sergei Roumiantsev 61 0.8× 76 1.3× 90 1.9× 87 2.4× 66 2.0× 6 354
Murat Elli 51 0.7× 31 0.5× 34 0.7× 37 1.0× 35 1.1× 29 199
Jean Charles Ruiz 56 0.7× 37 0.6× 26 0.6× 63 1.7× 75 2.3× 9 305
Aspasia Fotinou 76 1.0× 72 1.2× 34 0.7× 24 0.6× 7 0.2× 18 401
Takehiro Ohara 84 1.1× 30 0.5× 37 0.8× 19 0.5× 18 0.5× 23 339
Mehmet Akif Özdemir 29 0.4× 32 0.6× 29 0.6× 35 0.9× 78 2.4× 34 272
K. Kühn 56 0.7× 67 1.2× 67 1.4× 114 3.1× 13 0.4× 23 375

Countries citing papers authored by Eda Özaydın

Since Specialization
Citations

This map shows the geographic impact of Eda Özaydın's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Eda Özaydın with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eda Özaydın more than expected).

Fields of papers citing papers by Eda Özaydın

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eda Özaydın. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Eda Özaydın. The network helps show where Eda Özaydın may publish in the future.

Co-authorship network of co-authors of Eda Özaydın

This figure shows the co-authorship network connecting the top 25 collaborators of Eda Özaydın. A scholar is included among the top collaborators of Eda Özaydın based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Eda Özaydın. Eda Özaydın is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Özyürek, Hamìt, et al.. (2022). Homozygous SLC20A2 mutations cause congenital CMV infection-like phenotype. Acta Neurologica Belgica. 123(5). 1757–1761. 3 indexed citations
2.
Gündüz, Mehmet, et al.. (2021). Molecular and clinical findings of Turkish patients with hereditary fructose intolerance. Journal of Pediatric Endocrinology and Metabolism. 34(8). 1017–1022. 4 indexed citations
3.
Gündüz, Mehmet, Eda Özaydın, Ceyda Tuna Kırşaçlıoğlu, et al.. (2016). Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up. Indian Journal of Gastroenterology. 35(3). 236–241. 8 indexed citations
4.
Gündüz, Mehmet, Fatih Azık, Betül Tavil, et al.. (2016). Stepwise diet management in pediatric gastrointestinal graft versus host disease. The Turkish Journal of Pediatrics. 58(2). 145–151. 6 indexed citations
5.
Azkur, Dilek, et al.. (2016). Viral etiology in infants hospitalized for acute bronchiolitis.. PubMed. 56(6). 592–6. 9 indexed citations
6.
Gündüz, Mehmet, et al.. (2015). 3-HMG Coenzyme A Lyase Deficiency: Macrocephaly and Left Ventricular Noncompaction with a Novel Mutation. The Indian Journal of Pediatrics. 82(7). 645–648. 6 indexed citations
7.
Walsh, Meghan T., Jahangir Iqbal, Enza Di Leo, et al.. (2015). Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function. Circulation Cardiovascular Genetics. 8(5). 677–687. 22 indexed citations
8.
Ekici, Filiz, et al.. (2014). Reversible pulmonary arterial hypertension in cobalamin-dependent cobalamin C disease due to a novel mutation in the MMACHC gene. European Journal of Pediatrics. 173(12). 1707–1710. 29 indexed citations
9.
Özaydın, Eda, et al.. (2013). The Association Between Vitamin D Status and Recurrent Wheezing. The Indian Journal of Pediatrics. 80(11). 907–910. 11 indexed citations
10.
Özaydın, Eda, et al.. (2012). Differences in iron deficiency anemia and mean platelet volume between children with simple and complex febrile seizures. Seizure. 21(3). 211–214. 30 indexed citations
11.
Özaydın, Eda, et al.. (2012). Konjenital Glikozilasyon Bozukluğu Tip II. 6(1). 47–53. 1 indexed citations
12.
Özaydın, Eda, et al.. (2011). Febril Konvülziyonlu 1385 Vakanın Klinik Özellikleri ve Risk Faktörleri. Turkish Journal of Pediatric Disease. 5(1). 11–18. 1 indexed citations
13.
Özaydın, Eda, et al.. (2009). Management of central diabetes insipidus with oral desmopressin in a patient with ectrodactyly and cleft lip/palate (ECP) syndrome.. PubMed. 51(1). 89–93. 3 indexed citations
14.
Ünal, Sevim, Ayşe Esin Kibar, Eda Özaydın, Nilgün Karadağ, & Sevim Balcı. (2008). A new case of VACTERL association with congenital arachnoid cyst. Clinical Dysmorphology. 17(3). 221–222. 3 indexed citations
15.
Ünal, Sevim, et al.. (2008). İndirekt Hiperbilirubinemili Yenidoğanların Geriye Dönük OlarakDeğerlendirilmesi. 17(4). 223–229.
16.
Özaydın, Eda, et al.. (2007). Acute hemorrhagic pancreatitis due to the use of valproic acid in a child. European Journal of Paediatric Neurology. 12(2). 141–143. 7 indexed citations
17.
Durusoy, Çiçek, et al.. (2006). PHACES syndrome presenting as hemangiomas, sternal clefting and congenital ulcerations on the helices. The Journal of Dermatology. 33(3). 219–222. 10 indexed citations
18.
Özaydın, Eda, et al.. (2006). Nasal Cytology in the Diagnosis and Treatment of Sinusitis in Atopic and Nonatopic Children. The Journal of Otolaryngology. 35(4). 255–255. 3 indexed citations
19.
Çeliker, Reyhan, Serpil Bal, Ayşı̇n Bakkaloğlu, et al.. (2003). Factors playing a role in the development of decreased bone mineral density in juvenile chronic arthritis. Rheumatology International. 23(3). 127–129. 23 indexed citations
20.
Andıran, Nesibe, et al.. (2001). Mucocele of the anterior lingual salivary glands: from extravasation to an alarming mass with a benign course. International Journal of Pediatric Otorhinolaryngology. 61(2). 143–147. 29 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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